{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Callow B"],"funding":["American Heart Association","American Surgical Association Foundation","Vascular and Endovascular Surgery Society"],"pagination":["e183959"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11790032"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["10(2)"],"pubmed_abstract":["Abdominal aortic aneurysms (AAA) are a life-threatening cardiovascular disease for which there is a lack of effective therapy preventing aortic rupture. During AAA formation, pathological vascular remodeling is driven by vascular smooth muscle cell (VSMC) dysfunction and apoptosis, for which the mechanisms regulating loss of VSMCs within the aortic wall remain poorly defined. Using single-cell RNA-Seq of human AAA tissues, we identified increased activation of the endoplasmic reticulum stress response pathway, PERK/eIF2α/ATF4, in aortic VSMCs resulting in upregulation of an apoptotic cellular response. Mechanistically, we reported that aberrant TNF-α activity within the aortic wall induces VSMC ATF4 activation through the PERK endoplasmic reticulum stress response, resulting in progressive"],"journal":["JCI insight"],"pubmed_title":["Inhibition of vascular smooth muscle cell PERK/ATF4 ER stress signaling protects against abdominal aortic aneurysms."],"pmcid":["PMC11790032"],"funding_grant_id":["Early Career Investigator Award","23CDA1040660","AWD023254_ASA"],"pubmed_authors":["Davis FM","Xing X","Gallagher K","Joshi A","Mangum KD","Chattopadhyay A","Obi A","Callow B","He X","Milewicz DM","Juriga N","Gudjonsson J","O'Riordan MX"],"additional_accession":[]},"is_claimable":false,"name":"Inhibition of vascular smooth muscle cell PERK/ATF4 ER stress signaling protects against abdominal aortic aneurysms.","description":"Abdominal aortic aneurysms (AAA) are a life-threatening cardiovascular disease for which there is a lack of effective therapy preventing aortic rupture. During AAA formation, pathological vascular remodeling is driven by vascular smooth muscle cell (VSMC) dysfunction and apoptosis, for which the mechanisms regulating loss of VSMCs within the aortic wall remain poorly defined. Using single-cell RNA-Seq of human AAA tissues, we identified increased activation of the endoplasmic reticulum stress response pathway, PERK/eIF2α/ATF4, in aortic VSMCs resulting in upregulation of an apoptotic cellular response. Mechanistically, we reported that aberrant TNF-α activity within the aortic wall induces VSMC ATF4 activation through the PERK endoplasmic reticulum stress response, resulting in progressive","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Jan","modification":"2026-06-02T04:24:15.163Z","creation":"2025-04-19T16:22:22.808Z"},"accession":"S-EPMC11790032","cross_references":{"pubmed":["39846252"],"doi":["10.1172/jci.insight.183959"]}}